@article {1433,
	title = {Reaction of H2S with MoRu(CO)(6)(dppm)(2) to give H-2 and a bridged-sulfide product via hydrido-sulfhydryl intermediates (dppm = Ph2PCH2PPh2)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {84},
	number = {2},
	year = {2006},
	note = {ISI Document Delivery No.: 040YKTimes Cited: 2Cited Reference Count: 29},
	month = {Feb},
	pages = {330-336},
	type = {Article},
	abstract = {Oxidative addition of H2S to MoRu(CO)(6)(mu-dppm)(2) (1) at similar to 20 degrees C in toluene yields an isolable complex formulated as Mo(CO)(3)(mu-SH)(mu-CO)(mu-dppm)(2)RuH(CO) (2) via the possible intermediate Mo(CO)(3)(mu-H)(mu-CO)(mu-dppm)(2)Ru(SH)(CO) (4) (dppm = Ph2PCH2PPh2) that is detectable at lower temperatures. Over 2 days, species 2 in toluene loses H-2 (and CO) to yield the bridged-sulfide product, Mo(CO)(2)(mu-CO)(mu-S)(mu-dppm)(2)Ru(CO) (5) that is also formed directly from the reaction of 1 with elemental sulfur. The solid-state molecular structure of 5 is determined by X-ray crystallography. A further hydrido-sulfhydryl species, possibly Mo(CO)(3)(mu-SH)(mu-H)(mu-dppm)(2)Ru(CO)(2) (3), is in equilibrium with 2 at ambient temperature.},
	keywords = {bis(diphenylphosphino) methane, bis(diphenylphosphino)methane, BOND ACTIVATION, bridged-sulfide complex, carbonyl complexes, CHEMISTRY, COMPLEXES, hydrido-sulfhydryl species, HYDROGEN, HYDROGEN-SULFIDE, MECHANISTIC ASPECTS, METAL, MO, MOLYBDENUM, RECOVERY, ruthenium, sulfide, SULFUR-DIOXIDE},
	isbn = {0008-4042},
	url = {<Go to ISI>://000237417600031},
	author = {Khorasani-Motlagh, M. and Safari, N. and Pamplin, C. B. and Patrick, B. O. and James, Brian R.}
}
@article {1209,
	title = {Vanadium complexes with mixed O,S anionic ligands derived from maltol: Synthesis, characterization, and biological studies},
	journal = {Inorganic Chemistry},
	volume = {44},
	number = {8},
	year = {2005},
	note = {ISI Document Delivery No.: 916GWTimes Cited: 32Cited Reference Count: 45},
	month = {Apr},
	pages = {2678-2688},
	type = {Article},
	abstract = {Four mixed O,S binding bidentate ligand precursors derived from maltol (3-hydroxy-2-methyl-4-pyrone) have been chelated to vanadium to yield new bis(ligand)oxovanadium(IV) and tris(ligand)vanadium(III) complexes. The four ligand precursors include two pyranthiones, 3-hydroxy-2- m ethyl-4-pyranthione, commonly known as thiomaltol (Htma), and 2-ethyl-3-hydroxy-4-pyranthione, commonly known as ethylthiomaltol (Hetma), as well as two pyridinethiones, 3-hydroxy-2-methyl-4(H)-pyridinethione (Hmppt) and 3-hydroxy-1,2-dimethyi-4-pyridinethione (Hdppt). Vanadium complex formation was confirmed by elemental analysis, mass spectrometry, and IR and EPR (where possible) spectroscopies. The X-ray structure of oxobis(thiomaltolato)vanadium(IV),VO(tma)(2), was also determined; both cis and trans isomers were isolated in the same asymmetric unit. In both isomers, the two thiomaltolato ligands are arranged around the base of the square pyramid with the V=O linkage perpendicular; the vanadium atom is slightly displaced from the basal plane [V(1) = 0.656(3) angstrom, V(2) = 0.664(2) angstrom]. All of the new complexes were screened for insulin-enhancing effectiveness in streptozotocin-induced diabetes in rats, and VO(tma)2 was profiled metabolically for urinary vanadium and ligand clearance by GFAAS and ESIMS, respectively. The new vanadium complexes did not lower blood glucose levels acutely, possibly because of rapid dissociation and excretion.},
	keywords = {BIOCHEMISTRY, BIS(MALTOLATO)OXOVANADIUM(IV), COORDINATION CHEMISTRY, CRYSTAL-STRUCTURE, EPR, IN-VITRO, METAL, OXOVANADIUM(IV)},
	isbn = {0020-1669},
	url = {<Go to ISI>://000228374400018},
	author = {Monga, V. and Thompson, K. H. and Yuen, V. G. and Sharma, V. and Patrick, B. O. and McNeill, J. H. and Orvig, Chris}
}
@article {1209,
	title = {Vanadium complexes with mixed O,S anionic ligands derived from maltol: Synthesis, characterization, and biological studies},
	journal = {Inorganic Chemistry},
	volume = {44},
	number = {8},
	year = {2005},
	note = {ISI Document Delivery No.: 916GWTimes Cited: 32Cited Reference Count: 45},
	month = {Apr},
	pages = {2678-2688},
	type = {Article},
	abstract = {Four mixed O,S binding bidentate ligand precursors derived from maltol (3-hydroxy-2-methyl-4-pyrone) have been chelated to vanadium to yield new bis(ligand)oxovanadium(IV) and tris(ligand)vanadium(III) complexes. The four ligand precursors include two pyranthiones, 3-hydroxy-2- m ethyl-4-pyranthione, commonly known as thiomaltol (Htma), and 2-ethyl-3-hydroxy-4-pyranthione, commonly known as ethylthiomaltol (Hetma), as well as two pyridinethiones, 3-hydroxy-2-methyl-4(H)-pyridinethione (Hmppt) and 3-hydroxy-1,2-dimethyi-4-pyridinethione (Hdppt). Vanadium complex formation was confirmed by elemental analysis, mass spectrometry, and IR and EPR (where possible) spectroscopies. The X-ray structure of oxobis(thiomaltolato)vanadium(IV),VO(tma)(2), was also determined; both cis and trans isomers were isolated in the same asymmetric unit. In both isomers, the two thiomaltolato ligands are arranged around the base of the square pyramid with the V=O linkage perpendicular; the vanadium atom is slightly displaced from the basal plane [V(1) = 0.656(3) angstrom, V(2) = 0.664(2) angstrom]. All of the new complexes were screened for insulin-enhancing effectiveness in streptozotocin-induced diabetes in rats, and VO(tma)2 was profiled metabolically for urinary vanadium and ligand clearance by GFAAS and ESIMS, respectively. The new vanadium complexes did not lower blood glucose levels acutely, possibly because of rapid dissociation and excretion.},
	keywords = {BIOCHEMISTRY, BIS(MALTOLATO)OXOVANADIUM(IV), COORDINATION CHEMISTRY, CRYSTAL-STRUCTURE, EPR, IN-VITRO, METAL, OXOVANADIUM(IV)},
	isbn = {0020-1669},
	url = {<Go to ISI>://000228374400018},
	author = {Monga, V. and Thompson, K. H. and Yuen, V. G. and Sharma, V. and Patrick, B. O. and McNeill, J. H. and Orvig, Chris}
}
@article {569,
	title = {dlf complexes with uniform coordination geometry: Structural and magnetic properties of an LnNi2 core supported by a heptadentate amine phenol ligand},
	journal = {Inorganic Chemistry},
	volume = {42},
	number = {5},
	year = {2003},
	note = {ISI Document Delivery No.: 653EVTimes Cited: 20Cited Reference Count: 37},
	month = {Mar},
	pages = {1576-1583},
	type = {Article},
	abstract = {The synthesis and physical characterization of a series of lanthanide (Ln(III)) and nickel (Ni-II) mixed trimetallic complexes with the heptadentate (N4O3) amine phenol ligand H(3)trn [tris(2{\textquoteright}-hydroxybenzylaminoethyl)amine] has been accomplished in order to extend our understanding of how amine phenol ligands can be used to coaggregate d- and f-block metal ions and to investigate further the magnetic interaction between these ions. The one-pot reaction in methanol of stoichiometric amounts of H(3)trn with NiX2.6H(2)O (X = ClO4, NO3) followed by addition of the corresponding LnX(3).6H(2)O salt, and then base, produces complexes of the general formula [LnNi(2)(trn)(2)]X.nH(2)O.The complexes were characterized by a variety of analytical techniques. Crystals of five of the complexes were grown from methanol solutions and their structures were determined by X-ray analysis: [PrNi2(trn)(2)(CH3OH)]ClO4.4CH(3)-OH.H2O, [SmNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.2H(2)O, [TbNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.3H(2)O, [ErNi2(trn)(2)(CH3OH)]-NO3.6CH(3)OH, and [LuNi2(trn)(2)(CH3OH)]NO3.4.5CH(3)OH.1.5H(2)O. The [LnNi(2)(trn)(2)(CH3OH)](+) complex cation consists of two octahedral Ni-II ions, each of which is encapsulated by the ligand trn(3-) in an N4O2 coordination sphere with one phenolate O atom not bound to Ni-II. Each [Ni(trn)](-) unit acts as a tridentate ligand toward the Ln(III) ion via two bridging and one nonbridging phenolate donors. Remarkably, in all of the structurally characterized complexes, Ln(III) is seven-coordinate and has a flattened pentagonal bipyramidal geometry. Such uniform coordination behavior along the whole lanthanide series is rare and can perhaps be attributed to a mismatch between the geometric requirements of the bridging and nonbridging phenolate donors. Magnetic studies indicate that ferromagnetic exchange occurs in the Ni-II/Ln(II) complexes where Ln = Gd, Tb, Dy, Ho, or Er.},
	keywords = {AGENTS, BLOCK, CRYSTAL-STRUCTURE, DY, EXCHANGE, IONS, LANTHANIDE COMPLEXES, METAL, MOLECULES},
	isbn = {0020-1669},
	url = {<Go to ISI>://000181423000026},
	author = {Bayly, S. R. and Xu, Z. Q. and Patrick, B. O. and Rettig, S. J. and Pink, M. and Thompson, R. C. and Orvig, Chris}
}
@article {569,
	title = {dlf complexes with uniform coordination geometry: Structural and magnetic properties of an LnNi2 core supported by a heptadentate amine phenol ligand},
	journal = {Inorganic Chemistry},
	volume = {42},
	number = {5},
	year = {2003},
	note = {ISI Document Delivery No.: 653EVTimes Cited: 20Cited Reference Count: 37},
	month = {Mar},
	pages = {1576-1583},
	type = {Article},
	abstract = {The synthesis and physical characterization of a series of lanthanide (Ln(III)) and nickel (Ni-II) mixed trimetallic complexes with the heptadentate (N4O3) amine phenol ligand H(3)trn [tris(2{\textquoteright}-hydroxybenzylaminoethyl)amine] has been accomplished in order to extend our understanding of how amine phenol ligands can be used to coaggregate d- and f-block metal ions and to investigate further the magnetic interaction between these ions. The one-pot reaction in methanol of stoichiometric amounts of H(3)trn with NiX2.6H(2)O (X = ClO4, NO3) followed by addition of the corresponding LnX(3).6H(2)O salt, and then base, produces complexes of the general formula [LnNi(2)(trn)(2)]X.nH(2)O.The complexes were characterized by a variety of analytical techniques. Crystals of five of the complexes were grown from methanol solutions and their structures were determined by X-ray analysis: [PrNi2(trn)(2)(CH3OH)]ClO4.4CH(3)-OH.H2O, [SmNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.2H(2)O, [TbNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.3H(2)O, [ErNi2(trn)(2)(CH3OH)]-NO3.6CH(3)OH, and [LuNi2(trn)(2)(CH3OH)]NO3.4.5CH(3)OH.1.5H(2)O. The [LnNi(2)(trn)(2)(CH3OH)](+) complex cation consists of two octahedral Ni-II ions, each of which is encapsulated by the ligand trn(3-) in an N4O2 coordination sphere with one phenolate O atom not bound to Ni-II. Each [Ni(trn)](-) unit acts as a tridentate ligand toward the Ln(III) ion via two bridging and one nonbridging phenolate donors. Remarkably, in all of the structurally characterized complexes, Ln(III) is seven-coordinate and has a flattened pentagonal bipyramidal geometry. Such uniform coordination behavior along the whole lanthanide series is rare and can perhaps be attributed to a mismatch between the geometric requirements of the bridging and nonbridging phenolate donors. Magnetic studies indicate that ferromagnetic exchange occurs in the Ni-II/Ln(II) complexes where Ln = Gd, Tb, Dy, Ho, or Er.},
	keywords = {AGENTS, BLOCK, CRYSTAL-STRUCTURE, DY, EXCHANGE, IONS, LANTHANIDE COMPLEXES, METAL, MOLECULES},
	isbn = {0020-1669},
	url = {<Go to ISI>://000181423000026},
	author = {Bayly, S. R. and Xu, Z. Q. and Patrick, B. O. and Rettig, S. J. and Pink, M. and Thompson, R. C. and Orvig, Chris}
}
@article {745,
	title = {Side-on bridging coordination of N-2: Spectroscopic characterization of the planar Zr2N2 core and theoretical investigation of its butterfly distortion},
	journal = {Chemistry-a European Journal},
	volume = {9},
	number = {2},
	year = {2003},
	note = {ISI Document Delivery No.: 638VDTimes Cited: 14Cited Reference Count: 37},
	month = {Jan},
	pages = {520-530},
	type = {Article},
	abstract = {The vibrational and electronic structure of the side-on N-2-bridged Zr complex [{(P2N2)Zr}(2)(u-n(2):n(2)-N-2)] (P2N2=PhP(CH2SiMe2NSiMe2CH2)(2)PPh) were analyzed. The vibrational characterization of the planar Zr2N2 core was based on resonance Raman and infrared spectroscopy. In the Raman spectrum, the N-N stretching band is found at 775 cm(-1) with an isotope shift of 22 cm(-1). Due to its appearance in many overtones and combination modes, the metal-metal stretch is assigned to the peak at 295 cm(-1). The two ungerade modes of the Zr2N2 core were identified in the infrared spectrum. Based on these four vibrations of the Zr2N2 unit, a quantum chemical assisted normal coordinate analysis (OCA-NCA) was performed. The force constants for the N-N and Zr-N bonds were calculated to be 1.53 and 2.58 mdyn Angstrom(-1), respectively. The butterfly distortion of the Zr2N2 unit obtained in DFT geometry optimizations of planar side-on N-2-bridged Zr complexes was analyzed in more detail. It was found that on bending of the Zr2N2 core, the lone pairs of the axial amide ligands are rotated by 90degrees. The bent Zr2N2 unit is 11 kcal mol(-1) lower in energy than the planar core due to a more uniform distribution of electron density between the metal atoms and NZ and delocalization of electron density from the amide ligands to the Zr2N2 unit. The spectroscopic implications of this distortion are analyzed.},
	keywords = {<P2N2>ZR(MU-ETA(2)-N-2)ZR<P2N2>, coordination modes, CRYSTAL-STRUCTURE, DIHYDROGEN, DINITROGEN COMPLEX, DINITROGEN COMPLEXES, END-ON, EXCHANGE, METAL, MOLECULAR CALCULATIONS, NITROGEN, POTENTIALS, REDUCTION, SPECTROSCOPY, vibrational, ZIRCONIUM},
	isbn = {0947-6539},
	url = {<Go to ISI>://000180592000018},
	author = {Studt, F. and Morello, L. and Lehnert, N. and Fryzuk,Michael D. and Tuczek, F.}
}
@article {5197,
	title = {O-protonation of a terminal nitrosyl group to form an eta(1)-hydroxylimido ligand},
	journal = {Journal of the American Chemical Society},
	volume = {123},
	number = {33},
	year = {2001},
	note = {ISI Document Delivery No.: 463TWTimes Cited: 9Cited Reference Count: 26},
	month = {Aug},
	pages = {8143-8144},
	type = {Article},
	keywords = {CHEMISTRY, COMPLEXES, CRYSTAL-STRUCTURE, METAL, MOLYBDENUM, NITRIC-OXIDE, REACTIVITY, REDUCTION, TUNGSTEN},
	isbn = {0002-7863},
	url = {<Go to ISI>://000170494200032},
	author = {Sharp, W. B. and Legzdins,Peter and Patrick, B. O.}
}
@article {4833,
	title = {Removal of phenolic hydroxyl groups in lignin model compounds and its effect on photostability},
	journal = {Holzforschung},
	volume = {54},
	number = {2},
	year = {2000},
	note = {ISI Document Delivery No.: 301QHTimes Cited: 3Cited Reference Count: 24},
	pages = {127-132},
	type = {Article},
	abstract = {The phenolic hydroxyl groups in the lignin model compounds, 2-methoxy-4-propylphenol and 4-hydroxy-3-methoxyacetophenone, were removed by first converting the hydroxyl groups to the trifluoromethanesulfonates (triflates) and then cleaving the triflate substituents via catalytic hydrogen transfer. The products, 1-methoxy-3-propylbenzene and 3-methoxyacelophenone: were characterized by H-1 and C-13 NMR, mass spectrometry and elemental analyses. The effect of the removal of the phenolic groups on the photostability of the model compounds was evaluated by impregnating the compounds into Whatman filter paper sheets, and subjecting them to an accelerated yellowing experiment in a UV chamber. The removal of the phenolic groups resulted in a significant yellowing inhibition, with a higher photostabilizing effect than methylation or acetylation of the hydroxyl, particularly for the model compound without an alpha-carbonyl group.},
	keywords = {ACETYLATION, DEGRADATION, DEOXYGENATION, GROUPS, HYDROGENATION, LIGNIN MODEL COMPOUNDS, METAL, METHYLATION, phenolic hydroxyl, photostability yellowing, REDUCTION},
	isbn = {0018-3830},
	url = {<Go to ISI>://000086320500004},
	author = {Hu, Thomas Q. and Cairns, G. R. and James, Brian R.}
}
@article {4833,
	title = {Removal of phenolic hydroxyl groups in lignin model compounds and its effect on photostability},
	journal = {Holzforschung},
	volume = {54},
	number = {2},
	year = {2000},
	note = {ISI Document Delivery No.: 301QHTimes Cited: 3Cited Reference Count: 24},
	pages = {127-132},
	type = {Article},
	abstract = {The phenolic hydroxyl groups in the lignin model compounds, 2-methoxy-4-propylphenol and 4-hydroxy-3-methoxyacetophenone, were removed by first converting the hydroxyl groups to the trifluoromethanesulfonates (triflates) and then cleaving the triflate substituents via catalytic hydrogen transfer. The products, 1-methoxy-3-propylbenzene and 3-methoxyacelophenone: were characterized by H-1 and C-13 NMR, mass spectrometry and elemental analyses. The effect of the removal of the phenolic groups on the photostability of the model compounds was evaluated by impregnating the compounds into Whatman filter paper sheets, and subjecting them to an accelerated yellowing experiment in a UV chamber. The removal of the phenolic groups resulted in a significant yellowing inhibition, with a higher photostabilizing effect than methylation or acetylation of the hydroxyl, particularly for the model compound without an alpha-carbonyl group.},
	keywords = {ACETYLATION, DEGRADATION, DEOXYGENATION, GROUPS, HYDROGENATION, LIGNIN MODEL COMPOUNDS, METAL, METHYLATION, phenolic hydroxyl, photostability yellowing, REDUCTION},
	isbn = {0018-3830},
	url = {<Go to ISI>://000086320500004},
	author = {Hu, Thomas Q. and Cairns, G. R. and James, Brian R.}
}
@article {4855,
	title = {X-ray photoelectron spectroscopy studies of the stability of Al/Mg/PET interfaces},
	journal = {Surface Review and Letters},
	volume = {7},
	number = {3},
	year = {2000},
	note = {ISI Document Delivery No.: 356MBTimes Cited: 3Cited Reference Count: 33},
	month = {Jun},
	pages = {227-233},
	type = {Article},
	abstract = {The interfacial chemistry of an Al/Mg/PET sample, prepared by thermally evaporating first Mg and then Al on to a polyethyleneterephthalate (PET) film, was studied by X-ray photoelectron spectroscopy (XPS). The Mg/PET system showed two types of Mg species, namely an O-Mg-C complex, from reaction with the carbonyl group on PET, and metal-like clusters. The deposition of Al results in intermetallic mixing, which is manifested by alloy formation and Mg enrichment at the surface. It appears that some Al atoms penetrate the Mg region to react with carbonyl groups in the PET and form an interfacial complex with O-Al-C bonding. The stability of this sample was studied on exposing it to air and then rinsing it with water. The metal overlayers are strongly modified by these treatments, although the bonding at the PET interface appears relatively unchanged.},
	keywords = {AL-MG ALLOYS, aluminum, conjugated polymers, LIGHT-EMITTING-DIODES, MAGNESIUM, METAL, POLY(P-PHENYLENE VINYLENE), POLYIMIDE INTERFACE, THIN-FILMS, XPS},
	isbn = {0218-625X},
	url = {<Go to ISI>://000089446100005},
	author = {Kono, M. and Wong, P. C. and Li, Y. S. and Mitchell, K. A. R.}
}
@article {4689,
	title = {Undercarboxylation of recombinant prothrombin revealed by analysis of gamma-carboxyglutamic acid using capillary electrophoresis and laser-induced fluorescence},
	journal = {Febs Letters},
	volume = {445},
	number = {2-3},
	year = {1999},
	note = {ISI Document Delivery No.: 175YCTimes Cited: 6Cited Reference Count: 37},
	month = {Feb},
	pages = {256-260},
	type = {Article},
	abstract = {The gamma-carboxyglutamic acid (Gla) content of several variants of human prothrombin has been measured by using capillary electrophoresis and laser-induced fluorescence (CE-LIF). Both plasma-derived prothrombin and recombinant prothrombin contain ten residues of Gla per molecule of protein. In contrast, a variant of human prothrombin (containing the second kringle domain of bovine prothrombin) was separated into two populations that differed in their Gla content. Direct measurement of the Gla content showed an association with the presence or absence of the calcium-dependent conformational change that is required for prothombinase function. Thus, the CE-LIF assay is useful in determining the carboxylation status of recombinant proteins. (C) 1999 Federation of European Biochemical Societies.},
	keywords = {baby hamster kidney, calcium, capillary electrophoresis, cell, EXPRESSION, FACTOR-X, gamma carboxy glutamic acid, GLUTAMIC-ACID, HUMAN PROTEIN-C, LASER-INDUCED FLUORESCENCE, METAL, PHOSPHOLIPID-BINDING-PROPERTIES, PROTHROMBIN, PURIFICATION, recombinant protein, RESIDUES, VITAMIN-K},
	isbn = {0014-5793},
	url = {<Go to ISI>://000079122800007},
	author = {Vo, H. C. and Britz-McKibbin, P. and Chen, D. D. Y. and MacGillivray, R. T. A.}
}
@article {4255,
	title = {Complementary use of capillary gas chromatography mass spectrometry (ion trap) and gas chromatography inductively coupled plasma mass spectrometry for the speciation of volatile antimony, tin and bismuth compounds in landfill and fermentation gases},
	journal = {Analyst},
	volume = {123},
	number = {5},
	year = {1998},
	note = {ISI Document Delivery No.: ZN568Times Cited: 40Cited Reference Count: 183rd International Symposium on Speciation of Trace Elements in Biological, Environmental and Toxicological SciencesSEP 15-19, 1997PORT DOUGLAS, AUSTRALIAUniv New S Wales, Natl Inst Occupat Hlth, McMaster Univ, Inst Environ \& Hlth, MAFF, CSL, Food Sci Lab},
	month = {May},
	pages = {815-820},
	type = {Proceedings Paper},
	abstract = {ICP-MS is very sensitive and has limited matrix effects when used as an element-specific detector for GC in order to identify volatile metal or metalloid species, GC-MS is not very sensitive or selective in the electron ionization (EI) mode, but provides molecular information about volatile species. In this work, an ion trap EI-MS-MS and an ICP-MS system were used as two different detectors for the same GC system to provide complementary information about volatile organometallic species in the complex matrices of landfill and sewage sludge fermentation gases. A simple robust GC separation method with cryotrapping was adequate for the separation of the different metal(loid) containing volatile compounds, and was directly coupled to the ICP-MS system, In addition, gas samples from this GC system were collected in evacuated vials. These fractions were further separated on a capillary column and detected in an ion trap mass spectrometer. For the first time, parent ions, fragmentation patterns, isotopic ratios for Sb and Sn, and MS-MS data were used to identify positively Me3Sb, Me4Sn and Et2Me2Sn in landfill gas and Me3Sb and Me3Bi in fermentation gas.},
	keywords = {ELEMENTS, fermentation gas, gas chromatography-inductively coupled, ion trap mass spectrometry, landfill gas, MASS SPECTROMETRY, METAL, MS, organometallics, ORGANOTIN COMPOUNDS, trimethylbismuthine, trimethylstibine, VOLATILE, WASTE DEPOSITS},
	isbn = {0003-2654},
	url = {<Go to ISI>://000073658900010},
	author = {Feldmann, J. and Koch, I. and Cullen, W. R.}
}
@article {3954,
	title = {A characterization of the gamma-glycidoxypropyltrimethoxysilane and aluminium interface by SIMS and XPS},
	journal = {Journal of Materials Science Letters},
	volume = {16},
	number = {20},
	year = {1997},
	note = {ISI Document Delivery No.: YD607Times Cited: 21Cited Reference Count: 14},
	month = {Oct},
	pages = {1675-1676},
	type = {Article},
	keywords = {COUPLING AGENTS, FILMS, ION MASS-SPECTROMETRY, METAL, OXIDE, POLYMER SURFACES, SILANES, STEEL},
	isbn = {0261-8028},
	url = {<Go to ISI>://A1997YD60700017},
	author = {Fang, J. and Flinn, B. J. and Leung, Y. L. and Wong, P. C. and Mitchell, K. A. R. and Foster, T.}
}
@article {2964,
	title = {ATOMIC MASS-SPECTROMETRY},
	journal = {Applied Spectroscopy},
	volume = {48},
	number = {11},
	year = {1994},
	note = {ISI Document Delivery No.: PW171Times Cited: 7Cited Reference Count: 65},
	month = {Nov},
	pages = {A12-A18},
	type = {Review},
	keywords = {DISCHARGE SOURCE, ELECTROTHERMAL VAPORIZATION, ELEMENTAL ANALYSIS, GEOLOGICAL-MATERIALS, ICP-MS, inductively coupled plasma, LASER, METAL, MICROPROBE, SAMPLE INTRODUCTION, SOLIDS},
	isbn = {0003-7028},
	url = {<Go to ISI>://A1994PW17100002},
	author = {Blades, M. W.}
}
@article {7302,
	title = {ORGANOMETALLIC OXO CHEMISTRY .4. REACTIVITY OF CP-ASTERISK-W(O)2(CH2SIME3) TOWARD PARA-TOLYL ISOCYANATE - CYCLOADDITION REACTIONS OF TUNGSTEN-OXO AND TUNGSTEN-IMIDO LINKAGES},
	journal = {Organometallics},
	volume = {11},
	number = {9},
	year = {1992},
	note = {ISI Document Delivery No.: JN066Times Cited: 50Cited Reference Count: 40},
	month = {Sep},
	pages = {3104-3110},
	type = {Article},
	abstract = {{Treatment of CP*W(O)2(CH2SiMe3) with p-tolyl isocyanate under appropriate experimental conditions leads to the formation of Cp*W(O)(NC6H4-p-Me)(CH2SiMe3) (1), Cp*W(NC6H4-p-Me)2(CH2SiMe3) (2), or Cp*W(NC6H4-P-Me)[N(C6H4-P-Me)C(O)N(C6H4-P-Me)](CH2SiMe3) (3). Each of the complexes 1-3 is derived in a sequential manner from its precursor by incorporation of an additional p-tolyl isocyanate fragment or molecule. The spectroscopic properties of these organometallic imido complexes are consistent with their possessing three-legged (1 and 2) and four-legged (3) piano-stool molecular structures. These conclusions have been confirmed by single-crystal X-ray crystallographic analyses of 2 and 3. Crystal data for 2: triclinic},
	keywords = {ACTIVATION, AMIDO, AMMOXIDATION, COMPLEXES, LIGANDS, METAL, MOLYBDENUM, OXIDATION, propylene, SULFIDO},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1992JN06600027},
	author = {Legzdins,Peter and Phillips, E. C. and Rettig, S. J. and Trotter, J. and Veltheer, J. E. and Yee, V. C.}
}
@article {7302,
	title = {ORGANOMETALLIC OXO CHEMISTRY .4. REACTIVITY OF CP-ASTERISK-W(O)2(CH2SIME3) TOWARD PARA-TOLYL ISOCYANATE - CYCLOADDITION REACTIONS OF TUNGSTEN-OXO AND TUNGSTEN-IMIDO LINKAGES},
	journal = {Organometallics},
	volume = {11},
	number = {9},
	year = {1992},
	note = {ISI Document Delivery No.: JN066Times Cited: 50Cited Reference Count: 40},
	month = {Sep},
	pages = {3104-3110},
	type = {Article},
	abstract = {{Treatment of CP*W(O)2(CH2SiMe3) with p-tolyl isocyanate under appropriate experimental conditions leads to the formation of Cp*W(O)(NC6H4-p-Me)(CH2SiMe3) (1), Cp*W(NC6H4-p-Me)2(CH2SiMe3) (2), or Cp*W(NC6H4-P-Me)[N(C6H4-P-Me)C(O)N(C6H4-P-Me)](CH2SiMe3) (3). Each of the complexes 1-3 is derived in a sequential manner from its precursor by incorporation of an additional p-tolyl isocyanate fragment or molecule. The spectroscopic properties of these organometallic imido complexes are consistent with their possessing three-legged (1 and 2) and four-legged (3) piano-stool molecular structures. These conclusions have been confirmed by single-crystal X-ray crystallographic analyses of 2 and 3. Crystal data for 2: triclinic},
	keywords = {ACTIVATION, AMIDO, AMMOXIDATION, COMPLEXES, LIGANDS, METAL, MOLYBDENUM, OXIDATION, propylene, SULFIDO},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1992JN06600027},
	author = {Legzdins,Peter and Phillips, E. C. and Rettig, S. J. and Trotter, J. and Veltheer, J. E. and Yee, V. C.}
}
@article {6990,
	title = {ORGANOMETALLIC NITROSYL CHEMISTRY .48. REACTIVITIES OF REPRESENTATIVE CYCLOPENTADIENYL ETA-4-TRANS-DIENE NITROSYL COMPLEXES OF MOLYBDENUM TOWARD ACETONE},
	journal = {Organometallics},
	volume = {10},
	number = {12},
	year = {1991},
	note = {ISI Document Delivery No.: GV093Times Cited: 20Cited Reference Count: 31},
	month = {Dec},
	pages = {4021-4030},
	type = {Article},
	abstract = {{When CpMo(NO)(eta-4-trans-butadiene) (Cp = eta-5-C5H5) is treated with acetone, a ligand-coupling reaction occurs to form two complexes having the composition CpMo(NO)(eta-4-CH2CHCHCH2CMe2O), one in which the allyl portion of the coupled ligand is endo (1A) and one in which the allyl is exo (1B) with respect to the Cp ligand. Complete structural assignment of 1A and 1B has been effected by using NMR spectroscopic methods. Similar treatment of Cp*Mo(NO)(eta-4-trans-butadiene) (Cp* = eta-5-C5Me5) affords a single organometallic product, 2, which is the Cp* analogue of 1A. The coupling reaction between CpMo(NO)(eta-4-trans-2,5-dimethyl-2,4-hexadiene) and acetone is fairly rapid, the initial products being the endo-allyl (3A) and exo-allyl (3B) complexes. The endo isomer, however, converts quickly and irreversibly to the exo-allyl isomer. If the latter reaction is left for 15 h at ambient conditions, then 3B and [CpMo(NO)]3(mu-2-eta-2-eta-1-O-CMe2)3, which is isolable as a THF solvate (4), are the only organometallic species present in the final reaction mixture. All new complexes isolated during this work have been fully characterized by conventional methods, and crystal structure analyses have been performed on 2, 3B, and 4. Crystals of Cp*Mo(NO)(eta-4-endo-CH2CHCHCH2CMe2O) (2) are orthorhombic, P2(1)2(1)2(1), with a = 9.2465 (15) angstrom},
	keywords = {CARBONYLATION, DIENE COMPLEXES, INSERTION, LIGANDS, METAL},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1991GV09300017},
	author = {Christensen, N. J. and Legzdins,Peter and Trotter, J. and Yee, V. C.}
}
@article {6990,
	title = {ORGANOMETALLIC NITROSYL CHEMISTRY .48. REACTIVITIES OF REPRESENTATIVE CYCLOPENTADIENYL ETA-4-TRANS-DIENE NITROSYL COMPLEXES OF MOLYBDENUM TOWARD ACETONE},
	journal = {Organometallics},
	volume = {10},
	number = {12},
	year = {1991},
	note = {ISI Document Delivery No.: GV093Times Cited: 20Cited Reference Count: 31},
	month = {Dec},
	pages = {4021-4030},
	type = {Article},
	abstract = {{When CpMo(NO)(eta-4-trans-butadiene) (Cp = eta-5-C5H5) is treated with acetone, a ligand-coupling reaction occurs to form two complexes having the composition CpMo(NO)(eta-4-CH2CHCHCH2CMe2O), one in which the allyl portion of the coupled ligand is endo (1A) and one in which the allyl is exo (1B) with respect to the Cp ligand. Complete structural assignment of 1A and 1B has been effected by using NMR spectroscopic methods. Similar treatment of Cp*Mo(NO)(eta-4-trans-butadiene) (Cp* = eta-5-C5Me5) affords a single organometallic product, 2, which is the Cp* analogue of 1A. The coupling reaction between CpMo(NO)(eta-4-trans-2,5-dimethyl-2,4-hexadiene) and acetone is fairly rapid, the initial products being the endo-allyl (3A) and exo-allyl (3B) complexes. The endo isomer, however, converts quickly and irreversibly to the exo-allyl isomer. If the latter reaction is left for 15 h at ambient conditions, then 3B and [CpMo(NO)]3(mu-2-eta-2-eta-1-O-CMe2)3, which is isolable as a THF solvate (4), are the only organometallic species present in the final reaction mixture. All new complexes isolated during this work have been fully characterized by conventional methods, and crystal structure analyses have been performed on 2, 3B, and 4. Crystals of Cp*Mo(NO)(eta-4-endo-CH2CHCHCH2CMe2O) (2) are orthorhombic, P2(1)2(1)2(1), with a = 9.2465 (15) angstrom},
	keywords = {CARBONYLATION, DIENE COMPLEXES, INSERTION, LIGANDS, METAL},
	isbn = {0276-7333},
	url = {<Go to ISI>://A1991GV09300017},
	author = {Christensen, N. J. and Legzdins,Peter and Trotter, J. and Yee, V. C.}
}
